Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region
Chrom. | Start | End | TF Name | Source | Predicted site? | Tissue/Cell line | id | More |
---|---|---|---|---|---|---|---|---|
chr17 | 74837609 | 74837624 | TFAP2A | JASPAR | yes | 21300489 | ||
chr17 | 74837609 | 74837624 | TFAP2C | JASPAR | yes | 21300490 | ||
chr17 | 74837609 | 74837624 | TFAP2A | JASPAR | yes | 56029349 | ||
chr17 | 74837609 | 74837624 | TFAP2C | JASPAR | yes | 56029350 | ||
chr17 | 74837612 | 74837624 | TFAP2C | JASPAR | yes | 21300491 | ||
chr17 | 74837612 | 74837624 | TFAP2C | JASPAR | yes | 56029351 | ||
chr17 | 74837622 | 74837643 | ZNF263 | JASPAR | yes | 21300492 | ||
chr17 | 74837622 | 74837643 | ZNF263 | JASPAR | yes | 56029352 | ||
chr17 | 74837636 | 74837644 | SP1 | TRANSFAC | yes | 21300493 | ||
chr17 | 74837636 | 74837644 | SP1 | TRANSFAC | yes | 56029353 | ||
chr17 | 74837642 | 74837652 | ELK1 | JASPAR | yes | 21300494 | ||
chr17 | 74837642 | 74837652 | ERF | JASPAR | yes | 21300495 | ||
chr17 | 74837642 | 74837652 | ELK1 | JASPAR | yes | 56029354 | ||
chr17 | 74837642 | 74837652 | ERF | JASPAR | yes | 56029355 | ||
chr17 | 74837643 | 74837652 | ELK4 | JASPAR | yes | 21300496 | ||
chr17 | 74837643 | 74837652 | ELK4 | JASPAR | yes | 56029356 | ||
chr17 | 74837657 | 74837678 | ZNF263 | JASPAR | yes | 21300497 | ||
chr17 | 74837657 | 74837678 | ZNF263 | JASPAR | yes | 56029357 | ||
chr17 | 74837670 | 74837675 | ETS2 | TRANSFAC | yes | 21300498 | ||
chr17 | 74837670 | 74837675 | ETS2 | TRANSFAC | yes | 56029358 | ||
chr17 | 74837701 | 74837706 | ETS2 | TRANSFAC | yes | 21300499 | ||
chr17 | 74837701 | 74837706 | ETS2 | TRANSFAC | yes | 56029359 | ||
chr17 | 74837748 | 74837765 | RARA | JASPAR | yes | 21300500 | ||
chr17 | 74837748 | 74837765 | RARA | JASPAR | yes | 56029360 | ||
chr17 | 74837781 | 74837794 | NFKB1 | JASPAR | yes | 21300501 | ||
chr17 | 74837781 | 74837794 | NFKB1 | JASPAR | yes | 56029361 | ||
chr17 | 74837808 | 74837826 | RARA | JASPAR | yes | 21300502 | ||
chr17 | 74837808 | 74837826 | RARA | JASPAR | yes | 56029362 | ||
chr17 | 74837813 | 74837823 | SP1 | JASPAR | yes | 21300503 | ||
chr17 | 74837813 | 74837823 | SP1 | JASPAR | yes | 56029363 | ||
chr17 | 74837814 | 74837824 | SP1 | JASPAR | yes | 21300504 | ||
chr17 | 74837814 | 74837824 | SP1 | JASPAR | yes | 56029364 | ||
chr17 | 74837816 | 74837826 | ZNF740 | JASPAR | yes | 21300505 | ||
chr17 | 74837816 | 74837826 | ZNF740 | JASPAR | yes | 56029365 | ||
chr17 | 74837819 | 74837840 | ZNF263 | JASPAR | yes | 21300506 | ||
chr17 | 74837819 | 74837840 | ZNF263 | JASPAR | yes | 56029366 | ||
chr17 | 74837820 | 74837826 | SP1 | TRANSFAC | yes | 21300507 | ||
chr17 | 74837820 | 74837826 | SP1 | TRANSFAC | yes | 56029367 | ||
chr17 | 74837822 | 74837837 | HSF1 | JASPAR | yes | 21300508 | ||
chr17 | 74837822 | 74837837 | HSF1 | JASPAR | yes | 56029368 | ||
chr17 | 74837829 | 74837841 | HINFP | JASPAR | yes | 21300509 | ||
chr17 | 74837829 | 74837841 | HINFP | JASPAR | yes | 56029369 | ||
chr17 | 74837835 | 74837845 | ELK1 | JASPAR | yes | 21300510 | ||
chr17 | 74837835 | 74837845 | ELK1 | JASPAR | yes | 56029370 | ||
chr17 | 74837839 | 74837845 | ETS1 | JASPAR | yes | 21300511 | ||
chr17 | 74837839 | 74837845 | SPI1 | JASPAR | yes | 21300512 | ||
chr17 | 74837839 | 74837845 | ETS1 | JASPAR | yes | 56029371 | ||
chr17 | 74837839 | 74837845 | SPI1 | JASPAR | yes | 56029372 | ||
chr17 | 74837871 | 74837875 | H4TF2 | TRANSFAC | yes | 21300513 | ||
chr17 | 74837871 | 74837875 | H4TF2 | TRANSFAC | yes | 56029373 | ||
chr17 | 74837877 | 74837881 | LFA1 | TRANSFAC | yes | 21300514 | ||
chr17 | 74837877 | 74837881 | LFA1 | TRANSFAC | yes | 56029374 | ||
chr17 | 74837878 | 74837888 | ID4 | JASPAR | yes | 21300515 | ||
chr17 | 74837878 | 74837888 | TCF4 | JASPAR | yes | 21300516 | ||
chr17 | 74837878 | 74837888 | ID4 | JASPAR | yes | 56029375 | ||
chr17 | 74837878 | 74837888 | TCF4 | JASPAR | yes | 56029376 | ||
chr17 | 74837880 | 74837885 | USF2 | TRANSFAC | yes | 21300517 | ||
chr17 | 74837880 | 74837885 | USF2 | TRANSFAC | yes | 56029377 |
chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
---|---|---|---|---|---|---|---|
chr17 | 74837636 | rs573900518 | T | TC |
|
5067655 | |
chr17 | 74837643 | rs146846431 | C | A,T |
|
5067656 | |
chr17 | 74837643 | rs543047558 | C | CG |
|
5067657 | |
chr17 | 74837780 | rs75874847 | C | T | no | 5067658 | |
chr17 | 74837841 | rs75441148 | G | A,C,T |
|
5067659 |
Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
---|---|---|---|---|---|---|---|---|---|---|---|
chr17 | 74864538 | 74946475 | + | MGAT5B | ENSG00000167889.8 | 74864538 | 0.87 | 1.0 | 16296 | 73353 |
Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
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